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Spictra

EUDAMED

Class IIa (EU MDR)

Ref SPT-CK-03/2025-09Model CAUVARY MYSORE ADULT PACK

by Medihub Sciencetec Private Limited

Identity

Trade Name
SPICTRA EUDAMED
Device Name
Perfusion Custom Pack EUDAMED
Model / Reference
CAUVARY MYSORE ADULT PACK EUDAMED
SPT-CK-03/2025-09 EUDAMED

Identifiers

Primary DI / UDI-DI
08906172230646 EUDAMED
Basic UDI-DI
B-08906172230646 EUDAMED
EMDN Code
C03010101 EXTRACORPOREAL CIRCULATION CIRCUITS EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Spictra by Medihub Sciencetec Private Limited — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000007056
Authorised Representative
Meddevices Lifesciences B.V. NL-AR-000000594

Sources (1)

  • EUDAMED a550f55c-f43b-466e-b544-971c70d41456 61 fields · synced Jun 18, 2026